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Cellosaurus UOXFi003-C (CVCL_EE32)

[Text version]

Cell line name UOXFi003-C
Synonyms MK088-7
Accession CVCL_EE32
Resource Identification Initiative To cite this cell line use: UOXFi003-C (RRID:CVCL_EE32)
Comments From: University of Oxford; Oxford; United Kingdom.
Omics: Transcriptome analysis.
Derived from sampling site: Skin; dermis. Cell type=Fibroblast.
Sequence variations
  • Mutation; HGNC; 4177; GBA; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Heterozygous (EBiSC).
Disease Parkinson's disease (NCIt: C26845)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A8Y9 (MK088)
Sex of cell Male
Age at sampling 46Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections EBiSC; UOXFi003-C - Discontinued
ECACC; 66540392
Cell line databases/resources hPSCreg; UOXFi003-C
Biological sample resources BioSamples; SAMEA4454479
Encyclopedic resources Wikidata; Q54991442
Gene expression databases GEO; GSM2634093
GEO; GSM2644507
Entry history
Entry creation13-Jul-2016
Last entry update17-Mar-2022
Version number12